The Mantra TENS is an advanced and modern digital dual channel TENS unit featuring 12 built in and 2 customizable programs. Three different treatment modes provide maximum flexibility for pain relief.
TENS units help with a wide variety of pain and has an 80% efficacy rate. If you suffer from any type of pain, the Mantra TENS may be able to help.
Reliable, flexible and easy to use!
WARNING: Please seek advice from your therapist before using Stimulation devices
Features and Benefits
Suitable for all types of pain relief Digital Dual Channel 12 Built in programs for ease of use 2 Customizable constant mode programs Ability to lock the unit Records time in use and average current User friendly Compact, light and reliable
Conventional TENS or Normal Mode
This mode enables the user to select any rate between 2 Hz - 200 Hz and a pulse width between 50 µS - 300 µS. This is the most frequently used of the three modes. The most common selection is 80 Hz with a 200 µS pulse width.
Burst Mode This mode is comparable to the low rate TENS technique except that each low rate pulse is substituted for by a short BURST of 9 pulses (200 µS) at 150 Hz. It is a combination of conventional and low rate TENS. The burst mode is often referred to as acupuncture like TENS.
Modulation Mode This mode is designed to help prevent nerve accommodation that some patient's experience. It is achieved by continuously cycling the pulse width and rate.
Specifications
Dual Channel Digital TENS Unit 12 Built in programs including Burst, Modulated and Conventional TENS programs 2 Customizable constant mode programs LCD displays: Intensity, Rate, Pulse Width, Time and program Mode Time setting 4 hours for built in programs or up to 12 hours for customizable programs Constant Current (extends battery life) Range: Rate: 2 Hz - 200 Hz, Pulse Width: 50 µS to 300 µS Lock mode function for recording time in use and locking the units parameters Automatic switch off after 4 minutes if unit is not in use User friendly
All our products are manufactured in compliance with the Medical Device Directive MDD93/42/EEC under the supervision of SGS, Notified Body number 0120.
Suitable for all types of pain relief 
ISO13485:2003